READY! Product database and Activity tracking

Our regulatory database has been developed with a focus on pharmaceutical companies managing medicinal product information, activities, and related documents, in both EU and non-EU countries.

The web user interface supports collaboration among various departments or geographic locations.

READY! IDMP Product database is a web-based, innovative Regulatory Information Management system (RIMs) handling your organisation’s critical data in a single reference source.

READY! Product database provides:

  • Regulatory database storing information and status about human and veterinary products and APIs
  • Support for EU and non-EU regulatory procedures
  • Tracking of Activities
  • Tracking important dates and deadlines
  • Automatic monitoring of deadlines and sending alerts via email
  • Archiving important documents (MAs, commitments, SmPCs, PILs, etc.)
  • Archiving submissions in various formats, including eCTD and NeeS
  • ISO IDMP/Article 57 submissions
  • Organisations management
    • Manufactures (APIs, finished, intermediates, packaging, batch releasers)
    • Partners (co-development, in-licensing, out-licensing, etc.)
    • Distributors
  • Packaging info & storage conditions
  • Additional custom data

READY! is based on ISO IDMP standards and SPOR controlled vocabularies.

With our regulatory database your can efficiently plan, track, and monitor all activities and tasks in various departments. Automatic reminders and email alerts help users focus on their daily work and never miss deadlines.

READY! is a replacement for all those Excel spreadsheets that you are using across your company.

Using READY! is simple and users like it.